Benzene-free synthesis of catechol: Interfacing microbial and chemical catalysis

被引:71
作者
Li, WS [1 ]
Xie, DM [1 ]
Frost, JW [1 ]
机构
[1] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
关键词
D O I
10.1021/ja045148n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The toxicity of aromatics frequently limits the yields of their microbial synthesis. For example, the 5% yield of catechol synthesized from glucose by Escherichia coli WN1/pWL1.290A under fermentor-controlled conditions reflects catechol's microbial toxicity. Use of in situ resin-based extraction to reduce catechol's concentration in culture medium and thereby its microbial toxicity during its synthesis from glucose by E. coli WN1/pWL1.290A led to a 7% yield of catechol. Interfacing microbial with chemical synthesis was then explored where glucose was microbially converted into a nontoxic intermediate followed by chemical conversion of this intermediate into catechol. Intermediates examined include 3-dehydroquinate, 3-dehydroshikimate, and protocatechuate. 3-Dehydroquinate and 3-dehydroshikimate synthesized, respectively, by E. coli OP1.1/pJY1.216A and E coli KL3/pJY1.216A from glucose were extracted and then reacted in water heated at 290degreesC to afford catechol in overall yields from glucose of 10% and 26%, respectively. The problematic extraction of these catechol precursors from culture medium was subsequently circumvented by high-yielding chemical dehydration of 3-dehydroquinate and 3-dehydroshikimate in culture medium followed by extraction of the resulting protocatechuate. After reaction of protocatechuate in water heated at 290degreesC, the overall yields of catechol synthesized from glucose via chemical dehydration of 3-dehydroquinate and chemical dehydration of 3-dehydroshikimate were, respectively, 25% and 30%. Direct synthesis of protocatechuate from glucose using E. coli KL3/pWL2.46B followed by its extraction and chemical decarboxylation in water gave a 24% overall yield of catechol from glucose. In situ resin-based extraction of protocatechaute synthesized by E. coli KL3/pWL2.46B followed by chemical decarboxylation of this catechol percursor was then examined. This employment of both strategies for dealing with the microbial toxicity of aromatic products led to the highest overall yield with catechol synthesized in 43% overall yield from glucose.
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收藏
页码:2874 / 2882
页数:9
相关论文
共 44 条
[1]   Roles of water for chemical reactions in high-temperature water [J].
Akiya, N ;
Savage, PE .
CHEMICAL REVIEWS, 2002, 102 (08) :2725-2750
[2]   APPLICATION OF A PRACTICAL BIOCATALYTIC REDUCTION TO AN ENANTIOSELECTIVE SYNTHESIS OF THE 5H-2,3-BENZODIAZEPINE LY300164 [J].
ANDERSON, BA ;
HANSEN, MM ;
HARKNESS, AR ;
HENRY, CL ;
VICENZI, JT ;
ZMIJEWSKI, MJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (49) :12358-12359
[3]   Microbial synthesis of p-hydroxybenzoic acid from glucose [J].
Barker, JL ;
Frost, JW .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 76 (04) :376-390
[4]  
BARKER JL, 2000, Patent No. 6030819
[5]  
Campbell CJ, 1998, SCI AM, V278, P77
[6]   Aromatic inhibitors of dehydroquinate synthase: Synthesis, evaluation and implications for gallic acid biosynthesis [J].
Chandran, SS ;
Frost, JW .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (12) :1493-1496
[7]   ENVIRONMENTALLY COMPATIBLE SYNTHESIS OF CATECHOL FROM D-GLUCOSE [J].
DRATHS, KM ;
FROST, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (09) :2395-2400
[8]   SYNTHESIS USING PLASMID-BASED BIOCATALYSIS - PLASMID ASSEMBLY AND 3-DEOXY-D-ARABINO-HEPTULOSONATE PRODUCTION [J].
DRATHS, KM ;
FROST, JW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (04) :1657-1659
[9]   BIOCATALYTIC SYNTHESIS OF AROMATICS FROM D-GLUCOSE - THE ROLE OF TRANSKETOLASE [J].
DRATHS, KM ;
POMPLIANO, DL ;
CONLEY, DL ;
FROST, JW ;
BERRY, A ;
DISBROW, GL ;
STAVERSKY, RJ ;
LIEVENSE, JC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (10) :3956-3962
[10]   CARCINOGENICITY OF INHALED BENZENE IN CBA MICE [J].
FARRIS, GM ;
EVERITT, JI ;
IRONS, RD ;
POPP, JA .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1993, 20 (04) :503-507